Reprogramming of interceptive actions: time course of temporal corrections for unexpected target velocity change

The authors investigated the time course of reprogramming of the temporal dimension of motor acts in a task requiring interception of a moving target. The target moved at a constant velocity on a monitor screen; in part of the trials, target velocity was unexpectedly increased or decreased. Those modifications were produced at different moments during target displacement, leaving periods of time from 100 to 800 ms for movement timing correction. The authors assessed the effects of probability of target velocity change (25% vs. 50%), uncertainty about direction of velocity change (unidirectional vs. bidirectional), and direction of velocity change (increase vs. decrease). Analysis of 24 participants' arm acceleration showed that fast adjustments took place between 100 and 200 ms after target velocity change similarly for all uncertainty conditions. Analysis of temporal error indicated that the combination of high probability of target velocity change and certainty on direction of target velocity change led to the most successful movement timing reprogramming. For the other experimental conditions, temporal accuracy was still poor when a period of 800 ms was available for correction. Movement reprogramming was a continuous process that was more efficient for target velocity increase than for target velocity decrease.     

Experts in fast-ball sports reduce anticipation timing cost by developing inhibitory control

The present study was conducted to examine the relationship between expertise in movement correction and rate of movement reprogramming within limited time periods, and to clarify the specific cognitive processes regarding superior reprogramming ability in experts. Event-related potentials (ERPs) were recorded in baseball experts (n=7) and novices (n=7) while they completed a predictive task. The task was to manually press a button to coincide with the arrival of a moving target. The target moved at a constant velocity, and its velocity was suddenly decreased in some trials. Under changed velocity conditions, the baseball experts showed significantly smaller timing errors and a higher rate of timing reprogramming than the novices. Moreover, ERPs in baseball experts revealed faster central negative deflection and augmented frontal positive deflection at 200ms (N200) and 300ms (Pd300) after target deceleration, respectively. Following this, peak latency of the next positive component in the central region (P300b) was delayed. The negative deflection at 200ms, augmented frontal positive deflection, and late positive deflection at 300ms have been interpreted as reflecting stimulus detection, motor inhibition, and stimulus-response translation processes. Taken together, these findings suggest that the experts have developed movement reprogramming to avoid anticipation cost, and this is characterized by quick detection of target velocity change, stronger inhibition of the planned, incorrect response, and update of the stimulus-response relationship in the changed environment.     

Information entropy and the variability of space-time movement error

The authors investigated the effects of movement time and movement distance on the information entropy and variability of spatial and temporal error in a discrete aiming movement. In Experiment 1, the authors held movement distance (100 mm) constant and manipulated 11 movement times (300-800 ms) of 8 participants. In Experiment 2, the authors tested 6 movement distances at 2 given movement times (15-60 mm at 300 ms; 40-240 mm at 800 ms) in 8 participants. The variability and entropy for spatial error increased with average movement velocity, whereas the variability and entropy for temporal error decreased as a function of average movement velocity. The common variance between variable error and entropy averaged about 84% and 72% for spatial and temporal errors, respectively, suggesting that the probabilistic approach of entropy reveals features that are not present in the standard deviation index of variability. The findings provide further evidence that information entropy may be a useful single-index representation of variability in the movement speed-accuracy relation.     

Perception-action coupling and expertise in interceptive actions

The goal of this experiment was to show that expertise in interceptive actions can be explained by a shorter delay in movement regulation. In this contribution, we tested tennis experts and non-experts using a simulated interceptive task. The experimental device simulated linear motion of an object toward a target on a horizontal runway. Participants had to intercept the simulated moving object with their right hand holding a cart that could slide along a horizontal track perpendicular to the runway. Three different velocity conditions were used: a constant velocity condition that maintained the initial velocity (2m/s) constant until arriving on the target; the decelerated and accelerated velocity conditions, in which the velocity suddenly changed (400 ms before its arrival on the target) from 2 to 1m/s or 3m/s, respectively. Timing accuracy and movement correction after the unexpected velocity change were analysed. The experts were more accurate in the decelerative case (-29 and -124 ms respectively), in the accelerative case (69 and 116 ms respectively), but not in the constant velocity case (2 and 13 ms respectively). Findings can be explained by the shorter visuo-motor delay (VMD: the time required to adapt the movement to the new velocity) for the experts (162 ms) than for the non-experts (221 ms). This shorter VMD offers more time to adapt the interceptive movement to the new velocity. These results can be interpreted as an optimization of the perception-action coupling with expertise.     

Target velocity effects on manual interception kinematics

Participants generated manual interception movements toward a target cursor that moved across a computer screen. The target reached its peak velocity either during the first third, at the midpoint, or during the last third of the movement. In Experiment 1 the view of the target was available for either the first 316, 633, 950, or 1267 ms, after which it disappeared. Results showed that for all viewing conditions, the timing of the interception velocity was related to the temporal properties of the target's trajectory. In Experiment 2, when the portion of the target trajectory that was viewed was reversed (such that participants did not see the first 316, 633, 950, or 1267 ms of the trajectory, but instead saw only the later portions of the trajectory), there was no clear relationship between the target trajectory and the timing of the aiming trajectory. These results suggest that participants use visual information early in the target's trajectory to form a representation of the target motion that is used to facilitate manual interception.     

Impaired short temporal interval discrimination in a dyslexic adult

The ability to discriminate short temporal intervals was examined in a dyslexic adult (E.C.) and six matched controls. Listeners had to decide whether the second interval was shorter or longer than a standard (target) interval. Each interval was defined as the silent duration between two successive brief tones. Eight target intervals were used, ranging from 100 to 1,200 ms in duration. At each target interval, the differential threshold (DL) for duration was assessed, with the use of an adaptive psychophysical procedure. The results show that E.C.'s differential threshold values were much larger than those of controls. Moreover, the slope estimates covering the duration range from 100 to 800 ms indicated that in comparison to controls, E.C.'s differential threshold increased dramatically as the target duration increased. Thus her timing impairment becomes more pronounced with increasing duration. This timing deficit is consistent with other studies that have found temporal processing deficits associated with dyslexia.     

How the visual system detects changes in the direction of moving targets

To determine how the visual system represents information about change in target direction, we studied the detection of such change under conditions of varying stimulus certainty. Target direction was either held constant over trials or was allowed to vary randomly. When target direction was constant the observer could be certain about that stimulus characteristic; randomizing the target direction rendered the observer uncertain. We measured response times (RTs) to changes in target direction following initial trajectories of varying time and distance. In different conditions, the observer was uncertain about either the direction of the initial trajectory, or the direction of change or both. With brief initial trajectories in random directions, uncertainty about initial direction elevated RTs by 50 ms or more. When the initial trajectories were at least 500 ms, this directional uncertainty ceased to affect RTs; then, only uncertainty about the direction of change affected RTs. We discuss the implications of these results for (i) schemes by which the visual system might code directional change; (ii) the visual integration time for directional information; and (iii) adaptational processes in motion perception.     

Scalar timing without reference memory? Episodic temporal generalization and bisection in humans

Three experiments tested whether the scalar property of timing could occur when humans timed short durations under conditions in which it was unlikely that they developed reference memories of temporal "standards". Experiment 1 used an episodic version of a temporal generalization task where judgements were made of the potential equality of two durations presented on each trial. Unknown to the subject, one of these was always 200, 400, 600, or 800 ms, and the other was of variable duration. Temporal generalization gradients showed the scalar property of superimposition at standard values greater than 200 ms. Experiment 2 used a variant of the "roving bisection" method invented by Rodriguez-Girones and Kacelnik (1998) modified so that the scalar property of timing could be observed empirically. Data from bisection with short/long standard pairs of 100/400, 200/800, and 300/1,200 ms showed nearly perfect scalar-type superimposition. Experiment 3 again used episodic temporal generalization, but durations were never repeated and came from three distinct time ranges. Superimposition was found across these ranges except for the shortest visual stimuli timed. The data suggested that scalar timing could occur in humans in conditions where the formation of reference memories of temporal standards was highly improbable.     

Space-time accuracy of rapid movements

The space-time accuracy of an elbow flexion movement task was examined in two experiments over a range of motion extents (1 degrees through 100 degrees ) and short-duration movement times (100, 125, 150, and 400 ms). Nonlinear speed-accuracy functions emerged for both spatial and temporal error over all the movement conditions examined. The results showed that the timing error and spatial error had a high degree of complementarity as predicted by a space-time model of the speed-accuracy relation (Hancock & Newell, 1985). The findings confirm that the frame of reference for measuring movement error determines in part the error functions observed.     

Effects of Visual Error Timing on Smooth Pursuit Gain Adaptation in Humans

Smooth pursuit (SP) is one of the precise oculomotor behaviors when tracking a moving object. Adaptation of SP is based on a visual-error driven motor learning process associated with predictable changes in the visual environment. Proper timing of a sensory signal is an important factor for adaptation of fine motor control. In this study, we investigated whether visual error timing affects SP gain adaptation. An adaptive change in SP gain is produced experimentally by repeated trials of a step-ramp tracking with 2 different velocities (double-velocity paradigm). The authors used the double-velocity paradigm where target speed changes 400 or 800 ms after the target onset. The results show that SP gain changed in a certain time window following adaptation. The authors suggest that SP adaptation shown in this study is associated with timing control mechanisms.     

Modulation of anticipatory postural adjustments in the anticipation-coincidence task

This study was designed to (a) verify whether the time available for movement preparation and execution modulates anticipatory postural adjustments/focal movement coordination and (b) determine to what extent the coordination in an anticipation-coincidence (AC) timing task is specific. Ten subjects performed an arm-raising movement from standing position in the reaction time, self-initiated (SI), and AC conditions. In the latter condition, subjects had to synchronize movement initiation or the end of the movement to the passage of a visual mobile on a target. In AC trials, time to contact (TC), which is the time before the mobile reached the target, was varied (720, 1,200, 3,000 ms). Electromyography, kinetic, and kinematics data were collected. Results showed that the coordination patterns were modified by TC, the velocity of the mobile, and the condition in which the movement was executed. It also showed that the behavior in the AC condition came closest to the 1 observed in SI condition when TC increased. These results support the existence of different control modes triggered by the temporal pressure.     

Repetition priming effects from attended vs. ignored single words in a semantic categorization task

The present research examines priming effects from a centrally presented single-prime word to which participants were instructed to either attend or ignore. The prime word was followed by a single central target word to which participants made a semantic categorization (animate vs. inanimate) task. The main variables manipulated across experiments were attentional instructions (attend vs. ignore the prime word), presentation duration of the prime word (20, 50, 80 or 100 ms), prime-target stimulus onset asynchrony (SOA; 300 vs. 800 ms), and temporal presentation of instructions (before vs. after the prime word). The results showed (a) a consistent interaction between attentional instructions and repetition priming and (b) a qualitatively different ignored priming pattern as a function of prime duration: reduced positive priming (relative to the attend instruction) for prime exposures of 80 and 100 ms, and reliable negative priming for the shorter prime exposures of 20 and 50 ms. In addition (c), the differential priming pattern for attend and ignore trials was observed at a prime-target SOA of 800 ms (but not at a shorter 300-ms SOA) and only when instructions were presented before the prime word. Methodological and theoretical implications of the present findings for the extant negative priming literature are discussed.     

The effect of expectancy of a threatening event on time perception in human adults

Two experiments were conducted to investigate the effect of a threatening stimulus in human adults in a temporal bisection task. In Experiment 1, for two anchor duration conditions (400/800 vs. 800/1600 ms), the participants completed trials in which the probe duration was followed by an aversive stimulus or a nonaversive stimulus. The results showed that the duration was judged longer when the participants expected an aversive rather than a nonaversive stimulus. In Experiment 2, the effect of the temporal localization of the aversive stimulus was also tested, with the aversive stimulus being presented at the beginning or at the end of the probe duration. The results revealed a temporal overestimation in each condition compared to the trials in which no aversive stimulus was presented. Furthermore, the temporal overestimation was greater when the expectation for the forthcoming threatening stimulus was longer. This temporal overestimation is explained in terms of a speeding-up of the neural timing system in response to the increase in the arousal level produced by the expectation of a threatening stimulus.     

Timing and the Control of Rhythmic Upper-Limb Movements

Accurate timing of limb displacement is crucial for effective motor control. The authors examined the effects of movement velocity, duration, direction, added mass, and auditory cueing on timing, spatial, and trajectory variability of single- and multijoint rhythmic movements. During single-joint movements, increased velocity decreased timing and spatial variability, whereas increased movement duration increased timing variability but decreased spatial variability. For multijoint movements, regardless of condition, increasing velocity decreased joint timing, spatial, and trajectory variability, but all hand variabilities were unaffected by velocity, duration, load, or direction. Timing, spatial, and trajectory variability was greater at the shoulder compared with the elbow and minimal at the hand, supporting the notion that reaching movements are planned in hand space as opposed to joint space.     

Moving the Arm at Different Rates: Slow Movements are Avoided

Qualitative and quantitative changes characterize locomotion and rhythmic interlimb coordination at different speeds. Legs and hands do not move more or less quickly; they also adopt different relative coordination patterns. In the present article, the authors asked whether similar transitions occur for unimanual hand movements when speed is slowed below the preferred speed. Participants moved a handheld dowel back and forth between 2 large circular targets in time with a metronome at periods between 370 ms and 1667 ms. The authors analyzed the kinematics of participants’ movements at each period and found that proportional dwell time and number of peaks in the velocity profile increased as driving periods increased. Path lengths and peak velocities remained relatively constant for driving periods exceeding 800 ms. Participants made only gradual changes to their movement parameters, so that they went from a continuous mode to a more discrete mode of behavior for longer driving periods. Thus, unlike for rhythmic bimanual movements or locomotory patterns, there are quantitative but no clear qualitative changes for unimanual movements. The results suggest that participants tried to move close to their preferred tempo at different rates, and that they avoided moving slowly.     

The role of temporal unpredictability for process interference and code overlap in perception-action dual tasks

Two experiments explore interference in dual tasks. The first task required perceptual judgment of the movement direction (left vs right) of a briefly presented stimulus; the second task was a tone-discrimination reaction-time (RT) task. Participants reported their judgment at leisure. In 50% of the trials they were told to ignore the stimulus (no report). The directions of stimulus movement and response in the RT task could either be the same or different, establishing cross-task compatibility (CTC) relations. We varied the degree of temporal unpredictability by using two stimulus-onset asynchronies (SOA, 100 ms vs 1200 ms) for the task stimuli. In Experiment 1, SOA was varied randomly within blocks of trials in one group and between blocks in another group. In Experiment 2, only the short SOA was used in one group and only the long SOA in another group. In both experiments, we observed substantially longer RTs with the short compared with the long SOA, regardless of whether there was temporal certainty (blocked or constant SOA) or uncertainty (random SOA) about stimulus onset. We assume that the process of encoding into short-term memory in one task interferes with concurrent retrieval processes (i.e., response selection) in the other task. This process interference effect was strongly reduced in no-report trials. Furthermore, we found shorter RT in compatible than in incompatible trials. This CTC effect diminished with long SOA but occurred even in no-report trials, implying that it refers to an automatically activated and then decaying code that primes response selection in the RT task.     

不同SOA下视觉返回抑制对视听觉整合的调节作用

基于外源性线索-靶子范式, 采用2(线索-靶子间隔时间, stimulus onset asynchronies, SOA：400~600 ms、1000~1200 ms) × 3(目标刺激类型：视觉、听觉、视听觉) × 2(线索有效性：有效线索、无效线索)的被试内实验设计, 要求被试对目标刺激完成检测任务, 以考察视觉线索诱发的返回抑制(inhibition of return, IOR)对视听觉整合的调节作用, 从而为感知觉敏感度、空间不确定性及感觉通道间信号强度差异假说提供实验证据。结果发现：(1) 随SOA增长, 视觉IOR效应显著降低, 视听觉整合效应显著增强; (2) 短SOA (400~600 ms)时, 有效线索位置上的视听觉整合效应显著小于无效线索位置, 但长SOA (1000~1200 ms)时, 有效与无效线索位置上的视听觉整合效应并无显著差异。结果表明, 在不同SOA条件下, 视觉IOR对视听觉整合的调节作用产生变化, 当前结果支持感觉通道间信号强度差异假说。     

Predictive Pointing Movements and Saccades Toward a Moving Target

The authors investigated whether and, if so, how velocity information is used to control predictive manual pointing movements and saccades. Participants (N = 6) intercepted an occluded moving target as if it were still visible. They kept their eyes fixated while the target moved. The target traveled over a fixed distance and changed its velocity on the way. The presentation time of the final velocity was varied. Both the eye and the hand overshot the slow target and undershot the fast target, particularly when the duration of the final velocity was short. Thus, responses were biased in the direction of the target's initial velocity. The error seemed to arise because participants did not take their latency into account when aiming at the target. Instead, they strategically aimed farther ahead when the target was fast. Amplitude was also more related to the position of velocity change than to final velocity duration. Both findings suggest that target velocity is not extrapolated but that individuals add an increment to the position of velocity change.     

Coordination and timing of spine and hip joints during full body reaching tasks

Coupling of spine and hip joints during full body reaching tasks was investigated in 16 participants (8 male and 8 female) who performed reaching tasks at comfortable and fast-paced movement speeds to three targets located in a para-sagittal plane. The participants paused at target contact for 500ms and then returned to an upright posture. Three-dimensional joint motions of the spine and hip were recorded using an electromagnetic tracking device. We found an effect of movement phase (i.e., reach and return) on the onset timing of the spine and hip joints. For most target locations and movement speeds, spine motion onset preceded hip motion onset during the reaching phase of the movement task. In the reach phase, when averaged across all movement conditions, spine joint motion preceded hip joint motion by an average of 48.9ms. In contrast, in the return phase, hip joint motion preceded spine joint motion by an average of 63.0ms. Additionally, when participants were instructed to use either a knee flexion or knee extension strategy to perform the reaching tasks there was no effect of movement strategy on timing of the spine and hip. There was also no effect of target height on the spine-hip ratio, but as movement speed increased, the spine/hip ratio decreased for all target locations due primarily to an increase in hip joint excursion. The findings indicate clear differences in onset timing of the spine and hip joints during reaching tasks that necessitate some forward bending of the trunk and that onset timing is reversed for the return to an upright posture.     

The visual control of aimed hand movements to stationary and moving targets.

The present study attempted to determine if during short-duration movements visual feedback can be processed in order to make adjustments to changes in the environment. The effect that varying the importance of monitoring target position has on the relative importance of vision of hand and vision of target (Carlton 1981a; Whiting and Cockerill 1974) was also examined. Subjects performed short- (150 ms) and longer-duration (330 ms) aimed hand movements under four visual feedback conditions (lights-on/lights-off by target-on/target-off) to stationary and moving targets. For the lights-off and target-off conditions, the lights and target, respectively, were extinguished 50 ms after movement initiation. For all moving-target conditions, the target started to move as the movement was initiated. Subjects were able to process visual information in 165 ms, as movement endpoints were biased in the direction of target motion for movements of this duration. Removing visual feedback 50 ms after movement initiation did not alter this finding. Subjects performed equally well with target and lights on or off, independent of whether the target remained stationary or moved. Presumably, during the first 50 ms of the movement subjects received sufficient visual information to aid in movement control.